|
ENST00000395796.8:c.*1131C>T
|
ENSP00000379142.4:n.*1131C>T
|
|
|
ENST00000616242.5:c.*253C>T
|
ENSP00000482149.2:n.*253C>T
|
|
|
ENST00000683378.1:n.359C>T
|
|
|
|
ENST00000336642.9:c.167C>T
|
ENSP00000338009.5:p.Ala56Val
|
|
|
ENST00000345378.7:c.1136C>T
|
ENSP00000223366.2:p.Ala379Val
|
|
|
ENST00000403799.8:c.1133C>T
MANE Select
|
ENSP00000384247.3:p.Ala378Val
|
|
|
ENST00000671824.1:c.1196C>T
|
ENSP00000500264.1:p.Ala399Val
|
|
|
ENST00000672743.1:n.145C>T
|
|
|
|
ENST00000673284.1:c.1133C>T
|
ENSP00000499852.1:p.Ala378Val
|
|
|
ENST00000336642.8:c.185C>T
|
ENSP00000338009.4:p.Ala62Val
|
|
|
ENST00000345378.6:c.1136C>T
|
ENSP00000223366.2:p.Ala379Val
|
|
|
ENST00000395796.7:c.1130C>T
|
ENSP00000379142.3:p.Ala377Val
|
|
|
ENST00000403799.7:c.1133C>T
|
ENSP00000384247.3:p.Ala378Val
|
|
|
ENST00000437084.1:c.1082C>T
|
ENSP00000402840.1:p.Ala361Val
|
|
|
ENST00000459642.1:n.513C>T
|
|
|
|
ENST00000616242.4:c.1130C>T
|
ENSP00000482149.1:p.Ala377Val
|
|
|
NM_000162.3:c.1133C>T
|
NP_000153.1:p.Ala378Val
|
|
|
NM_033507.1:c.1136C>T
|
NP_277042.1:p.Ala379Val
|
|
|
NM_033508.1:c.1130C>T
|
NP_277043.1:p.Ala377Val
|
|
|
NM_000162.4:c.1133C>T
|
NP_000153.1:p.Ala378Val
|
|
|
NM_001354800.1:c.1133C>T
|
NP_001341729.1:p.Ala378Val
|
|
|
NM_001354801.1:c.122C>T
|
NP_001341730.1:p.Ala41Val
|
|
|
NM_001354802.1:c.-8C>T
|
NP_001341731.1:n.-8C>T
|
|
|
NM_001354803.1:c.167C>T
|
NP_001341732.1:p.Ala56Val
|
|
|
NM_033507.2:c.1136C>T
|
NP_277042.1:p.Ala379Val
|
|
|
NM_033508.2:c.1130C>T
|
NP_277043.1:p.Ala377Val
|
|
|
XM_024446707.1:c.-8C>T
|
XP_024302475.1:n.-8C>T
|
|
|
NM_000162.5:c.1133C>T
MANE Select
|
NP_000153.1:p.Ala378Val
|
|
|
NM_033507.3:c.1136C>T
|
NP_277042.1:p.Ala379Val
|
|
|
NM_033508.3:c.1130C>T
|
NP_277043.1:p.Ala377Val
|
|
|
NM_001354803.2:c.167C>T
|
NP_001341732.1:p.Ala56Val
|
|
